NM_000030.3(AGXT):c.489G>A (p.Leu163=) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Jan 21, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000974765.12
Allele description [Variation Report for NM_000030.3(AGXT):c.489G>A (p.Leu163=)]
NM_000030.3(AGXT):c.489G>A (p.Leu163=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 15, 2024